A novel telomeric (approximately 285 kb) α-thalassemia deletion leading to a phenotypically unusual HbH disease

Haematologica. 2010 May;95(5):850-1. doi: 10.3324/haematol.2009.018663. Epub 2009 Nov 30.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Female
  • Gene Deletion*
  • Hemoglobin H / genetics*
  • Humans
  • Phenotype*
  • Scoliosis / complications
  • Scoliosis / diagnosis
  • Scoliosis / genetics
  • Telomere / genetics*
  • alpha-Thalassemia / complications
  • alpha-Thalassemia / diagnosis
  • alpha-Thalassemia / genetics*

Substances

  • Hemoglobin H